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Evaluation of multi-assay algorithms for identifying individuals with recent HIV infection: HPTN 071 (PopART).
Grant-McAuley, Wendy; Klock, Ethan; Laeyendecker, Oliver; Piwowar-Manning, Estelle; Wilson, Ethan; Clarke, William; Breaud, Autumn; Moore, Ayana; Ayles, Helen; Kosloff, Barry; Shanaube, Kwame; Bock, Peter; Mandla, Nomtha; van Deventer, Anneen; Fidler, Sarah; Donnell, Deborah; Hayes, Richard; Eshleman, Susan H.
Affiliation
  • Grant-McAuley W; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Klock E; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Laeyendecker O; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Piwowar-Manning E; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, United States of America.
  • Wilson E; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Clarke W; Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Breaud A; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Moore A; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Ayles H; FHI360, Durham, North Carolina, United States of America.
  • Kosloff B; Zambart, University of Zambia School of Medicine, Lusaka, Zambia.
  • Shanaube K; Clinical Research Department, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Bock P; Zambart, University of Zambia School of Medicine, Lusaka, Zambia.
  • Mandla N; Clinical Research Department, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • van Deventer A; Zambart, University of Zambia School of Medicine, Lusaka, Zambia.
  • Fidler S; Desmond Tutu TB Center, Department of Paediatrics and Child Health, Stellenbosch University, Western Cape, South Africa.
  • Donnell D; Desmond Tutu TB Center, Department of Paediatrics and Child Health, Stellenbosch University, Western Cape, South Africa.
  • Hayes R; Desmond Tutu TB Center, Department of Paediatrics and Child Health, Stellenbosch University, Western Cape, South Africa.
  • Eshleman SH; Department of Infectious Disease, Imperial College London, London, United Kingdom.
PLoS One ; 16(12): e0258644, 2021.
Article in En | MEDLINE | ID: mdl-34919554
BACKGROUND: Assays and multi-assay algorithms (MAAs) have been developed for population-level cross-sectional HIV incidence estimation. These algorithms use a combination of serologic and/or non-serologic biomarkers to assess the duration of infection. We evaluated the performance of four MAAs for individual-level recency assessments. METHODS: Samples were obtained from 220 seroconverters (infected <1 year) and 4,396 non-seroconverters (infected >1 year) enrolled in an HIV prevention trial (HPTN 071 [PopART]); 28.6% of the seroconverters and 73.4% of the non-seroconverters had HIV viral loads ≤400 copies/mL. Samples were tested with two laboratory-based assays (LAg-Avidity, JHU BioRad-Avidity) and a point-of-care assay (rapid LAg). The four MAAs included different combinations of these assays and HIV viral load. Seroconverters on antiretroviral treatment (ART) were identified using a qualitative multi-drug assay. RESULTS: The MAAs identified between 54 and 100 (25% to 46%) of the seroconverters as recently-infected. The false recent rate of the MAAs for infections >2 years duration ranged from 0.2%-1.3%. The MAAs classified different overlapping groups of individuals as recent vs. non-recent. Only 32 (15%) of the 220 seroconverters were classified as recent by all four MAAs. Viral suppression impacted the performance of the two LAg-based assays. LAg-Avidity assay values were also lower for seroconverters who were virally suppressed on ART compared to those with natural viral suppression. CONCLUSIONS: The four MAAs evaluated varied in sensitivity and specificity for identifying persons infected <1 year as recently infected and classified different groups of seroconverters as recently infected. Sensitivity was low for all four MAAs. These performance issues should be considered if these methods are used for individual-level recency assessments.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: HIV Infections / Anti-HIV Agents / Seroconversion Type of study: Diagnostic_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: HIV Infections / Anti-HIV Agents / Seroconversion Type of study: Diagnostic_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Type: Article Affiliation country: United States